Journal Article10.1126/SCIENCE.AAC5560
Dietary antigens limit mucosal immunity by inducing regulatory T cells in the small intestine
Kwang Soon Kim,Sung-Wook Hong,Daehee Han,Jaeu Yi,Jisun Jung,Bo Gie Yang,Junyoung Lee,Minji Lee,Charles D. Surh,Charles D. Surh +9 more
TL;DR: It is demonstrated that under normal conditions, the vast majority of the small intestinal T cells called regulatory T cells are induced by dietary antigens from solid foods, and these pTreg cells have a limited life span, are distinguishable from microbiota-induced pT Reg cells, and repress underlying strong immunity to ingested protein antIGens.
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Abstract: Dietary antigens are normally rendered nonimmunogenic through a poorly understood "oral tolerance" mechanism that involves immunosuppressive regulatory T (Treg) cells, especially Treg cells induced from conventional T cells in the periphery (pTreg cells). Although orally introducing nominal protein antigens is known to induce such pTreg cells, whether a typical diet induces a population of pTreg cells under normal conditions thus far has been unknown. By using germ-free mice raised and bred on an elemental diet devoid of dietary antigens, we demonstrated that under normal conditions, the vast majority of the small intestinal pTreg cells are induced by dietary antigens from solid foods. Moreover, these pTreg cells have a limited life span, are distinguishable from microbiota-induced pTreg cells, and repress underlying strong immunity to ingested protein antigens.
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References
Induced CD4+Foxp3+ Regulatory T Cells in Immune Tolerance
TL;DR: It is speculated that the different origin of iTreg cells (noninflammatory versus inflammatory) results in distinct properties, including their stability, which could contribute to their stability in the context of immunological tolerance.
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Intestinal Microbial Diversity during Early-Life Colonization Shapes Long-Term IgE Levels
TL;DR: It is reported that germ-free mice and those with low-diversity microbiota develop elevated serum IgE levels in early life and appropriate intestinal microbial stimuli during early life are critical for inducing an immunoregulatory network that protects from induction of IgE at mucosal sites.
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In vivo equilibrium of proinflammatory IL-17+ and regulatory IL-10+ Foxp3+ RORγt+ T cells
Matthias Lochner,Lucie Peduto,Marie Cherrier,Shinichiro Sawa,Francina Langa,Rosa Varona,Dieter Riethmacher,Mustapha Si-Tahar,James P. Di Santo,Gérard Eberl +9 more
TL;DR: It is reported here that potentially antagonistic proinflammatory IL-17–producing and regulatory Foxp3+ RORγt+ T cells coexist and are tightly controlled, suggesting that a perturbed equilibrium in RORαβ cells might lead to decreased immunoreactivity or, in contrast, to pathological inflammation.
Oral tolerance in the absence of naturally occurring Tregs
Daniel Mucida,Nino Kutchukhidze,Agustin Erazo,Momtchilo Russo,Juan J. Lafaille,Maria A. Curotto de Lafaille +5 more
TL;DR: Using a mouse model of hyper-IgE and asthma, it is found that oral tolerance could be effectively induced in the absence of naturally occurring thymus-derived Tregs and effector Th2 cells displaying the same antigen specificity.
A requisite role for induced regulatory T cells in tolerance based on expanding antigen receptor diversity.
Dipica Haribhai,Jason B. Williams,Shuang Jia,Derek W. Nickerson,Erica G. Schmitt,Brandon Edwards,Jennifer Ziegelbauer,Maryam Yassai,Shun Hwa Li,Lance M. Relland,Petra Wise,A. W. Chen,Yu Qian Zheng,Pippa Simpson,Jack Gorski,Nita H. Salzman,Martin J. Hessner,Talal A. Chatila,Calvin B. Williams +18 more
TL;DR: In adoptive transfer immunotherapy of newborn Foxp3-deficient mice, iTreg cells are an essential nonredundant regulatory subset that supplements nTreg cells in part by expanding TCR diversity within regulatory responses.
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